CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 150 enrolled
Drug / intervention
HL036 ophthalmic solution +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03334539
NCT03334539Phase 2Completed

A Phase 2, Multicenter, Randomized, Double-Masked and Placebo-Controlled Study Evaluating the Efficacy of Two Concentrations (0.10%, 0.25%) of HL036 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye

HanAll BioPharma Co., Ltd.·interventional·Posted Nov 7, 2017·Updated Mar 7, 2024

In Brief

A Phase 2 clinical trial evaluating HL036 ophthalmic solution and Placebo vehicle solution for Dry Eye. Completed, enrolled 150 participants across 2 sites.

Detailed Summary

The objective of this study was to compare the safety and efficacy of 0.10% and 0.25% HL036 Ophthalmic Solutions to placebo for the treatment of the signs and symptoms of dry eye.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedNov 7, 2017
Enrollment StartNov 5, 2017
Primary CompletionApr 9, 2018
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 8.7 years ago

Interventions

HL036 ophthalmic solutionbiological

HL036 ophthalmic solution

Placebo vehicle solutionother

Placebo vehicle solution